生物年龄加速,遗传易感性,以及发生眼风险
Wei-Qi Song1, Wen-Fang Zhong1, Zhi-Hao Li1
1Department of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China.
Investigative ophthalmology & visual science
|April 17, 2025
概括
生物衰老加速增加了玻璃眼风险,特别是在那些具有高遗传倾向的人群中. 这项研究没有发现因果关系,强调需要进一步调查老龄化与眼睛健康之间的关联.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 是一个遗传学.
- 衰老研究研究 衰老研究
背景情况:
- 玻璃眼是导致不可逆转失明的主要原因.
- 生物年龄与时间年龄不同,反映了生理衰退.
- 了解影响眼风险的因素对于早期检测和预防至关重要.
研究的目的:
- 评估生物衰老加快和新发眼之间的联系.
- 为了确定遗传倾向是否会改变这种关联.
- 使用孟德尔随机化探索潜在的因果关系.
主要方法:
- 利用了来自318,556名没有基线玻璃眼患者的英国生物库数据.
- 使用Klemera-Doubal方法计算生物年龄 (KDM-BA) 和PhenoAge算法计算生物年龄.
- 采用考克斯回归和门德尔随机化来分析与遗传风险的关联和相互作用.
主要成果:
- 生物年龄加速与高眼风险相关 (例如,5年加速:HR 1.12 KDM-BA,1.09 PhenoAge).
- 生物年龄较高的参与者表现出更高的玻璃眼风险.
- 遗传风险显著改变了这种关联,在具有高遗传风险的生物老年人中风险最高 (例如,HR 2.33 KDM-BA).
结论:
- 生物衰老的加速与增加的玻璃眼病发病率有关.
- 遗传风险在这种关系中起着改变作用.
- 没有发现因果关系,因此需要对潜在机制进行进一步的研究.
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